Variant report

Variant	nsv1017049
Chromosome Location	chr8:4567338-4654658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:159)
CpG islands
(count:610)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:159 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:4593306-4593480	K562	blood:	n/a	n/a
2	CEBPB	chr8:4613708-4613813	A549	lung:	n/a	n/a
3	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr8:4573370-4573868	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr8:4644680-4644748	Pancreas_OC	pancreas:	n/a	n/a
6	CTCF	chr8:4644640-4644790	GM12872	blood:	n/a	n/a
7	CTCF	chr8:4644640-4644790	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr8:4644647-4644806	GM12891	blood:	n/a	n/a
9	CTCF	chr8:4644660-4644810	GM12864	blood:	n/a	n/a
10	CTCF	chr8:4644620-4644770	SAEC	small airway:	n/a	n/a
11	CTCF	chr8:4644640-4644790	GM12868	blood:	n/a	n/a
12	CTCF	chr8:4612266-4612290	GM13976	blood:	n/a	n/a
13	CTCF	chr8:4644640-4644790	GM12865	blood:	n/a	n/a
14	CTCF	chr8:4644600-4644750	GM12866	blood:	n/a	n/a
15	CTCF	chr8:4644600-4644750	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr8:4644700-4644850	HRE	kidney:	n/a	n/a
17	CTCF	chr8:4644672-4644761	GM13977	blood:	n/a	n/a
18	CTCF	chr8:4644640-4644790	HepG2	liver:	n/a	n/a
19	CTCF	chr8:4644611-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:4644600-4644750	GM12873	blood:	n/a	n/a
21	CTCF	chr8:4644680-4644830	GM12871	blood:	n/a	n/a
22	CTCF	chr8:4644640-4644790	HEK293	kidney:	n/a	n/a
23	CTCF	chr8:4644660-4644810	K562	blood:	n/a	n/a
24	CTCF	chr8:4644620-4644770	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr8:4644580-4644730	A549	lung:	n/a	n/a
26	CTCF	chr8:4644540-4644690	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr8:4573639-4573761	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:4644591-4644910	K562	blood:	n/a	n/a
29	CTCF	chr8:4628455-4628505	LNCaP	prostate:	n/a	n/a
30	CTCF	chr8:4644584-4644870	K562	blood:	n/a	n/a
31	CTCF	chr8:4644660-4644810	GM12865	blood:	n/a	n/a
32	CTCF	chr8:4644660-4644810	HepG2	liver:	n/a	n/a
33	CTCF	chr8:4644680-4644830	GM12867	blood:	n/a	n/a
34	CTCF	chr8:4644620-4644770	GM12872	blood:	n/a	n/a
35	CTCF	chr8:4644700-4644850	GM12875	blood:	n/a	n/a
36	CTCF	chr8:4644680-4644830	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr8:4644640-4644790	GM12874	blood:	n/a	n/a
38	CTCF	chr8:4650026-4650077	ProgFib	skin:	n/a	n/a
39	CTCF	chr8:4632207-4632286	Lung_OC	lung:	n/a	n/a
40	CTCF	chr8:4571745-4571776	Fibrobl	skin:	n/a	n/a
41	CTCF	chr8:4644658-4644814	Gliobla	brain:	n/a	n/a
42	CTCF	chr8:4644647-4644651	HepG2	liver:	n/a	n/a
43	CTCF	chr8:4644600-4644750	SAEC	small airway:	n/a	n/a
44	CTCF	chr8:4644600-4644750	GM12871	blood:	n/a	n/a
45	CTCF	chr8:4644642-4644821	K562	blood:	n/a	n/a
46	CTCF	chr8:4644625-4644807	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr8:4644650-4644795	LNCaP	prostate:	n/a	n/a
48	CTCF	chr8:4644640-4644790	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr8:4644646-4644815	A549	lung:	n/a	n/a
50	CTCF	chr8:4644660-4644810	GM12869	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4601579-4601629	H1-hESC	embryonic stem cell:	embryo
2	chr8:4601508-4601558	NHDF-neo	bronchial:	n/a
3	chr8:4644719-4644769	PANC-1	pancreas:	n/a
4	chr8:4601579-4601629	SAEC	small airway:	n/a
5	chr8:4601508-4601558	HEEpiC	esophagus:	n/a
6	chr8:4583355-4583405	NB4	blood:	n/a
7	chr8:4617087-4617137	SK-N-MC	brain:	n/a
8	chr8:4644719-4644769	Hepatocyte	liver:	n/a
9	chr8:4629524-4629574	HAEpiC	amniotic membrane:	n/a
10	chr8:4583386-4583436	NHDF-neo	bronchial:	n/a
11	chr8:4637584-4637634	HUVEC	blood vessel:	n/a
12	chr8:4583355-4583405	AG09319	gingival:	n/a
13	chr8:4644739-4644789	HNPCEpiC	eye:	n/a
14	chr8:4637584-4637634	H1-hESC	embryonic stem cell:	embryo
15	chr8:4601579-4601629	SK-N-SH	brain:	n/a
16	chr8:4637584-4637634	HRCEpiC	kidney:	n/a
17	chr8:4644719-4644769	AG09319	gingival:	n/a
18	chr8:4617087-4617137	HCM	heart:	n/a
19	chr8:4573688-4573738	HCT-116	colon:	n/a
20	chr8:4583355-4583405	BE2_C	brain:	n/a
21	chr8:4601508-4601558	T-47D	breast:	n/a
22	chr8:4637584-4637634	AG09309	skin:	n/a
23	chr8:4629524-4629574	RPTEC	kidney:	n/a
24	chr8:4573688-4573738	ECC-1	luminal epithelium:	n/a
25	chr8:4629524-4629574	MCF10A-Er-Src	breast:	n/a
26	chr8:4617087-4617137	MCF10A-Er-Src	breast:	n/a
27	chr8:4629524-4629574	HRCEpiC	kidney:	n/a
28	chr8:4644719-4644769	SK-N-MC	brain:	n/a
29	chr8:4629524-4629574	GM06990	blood:	n/a
30	chr8:4637584-4637634	ProgFib	skin:	n/a
31	chr8:4583386-4583436	SKMC	muscle:	n/a
32	chr8:4583386-4583436	HEEpiC	esophagus:	n/a
33	chr8:4583386-4583436	MCF10A-Er-Src	breast:	n/a
34	chr8:4583386-4583436	ovcar-3	ovarian:	n/a
35	chr8:4601508-4601558	ovcar-3	ovarian:	n/a
36	chr8:4583355-4583405	T-47D	breast:	n/a
37	chr8:4617087-4617137	ovcar-3	ovarian:	n/a
38	chr8:4573688-4573738	GM12878	blood:	n/a
39	chr8:4644719-4644769	HepG2	liver:	n/a
40	chr8:4629524-4629574	HEK293	kidney:	embryo
41	chr8:4629524-4629574	HEEpiC	esophagus:	n/a
42	chr8:4637584-4637634	HIPEpiC	eye:	n/a
43	chr8:4644739-4644789	PFSK-1	brain:	n/a
44	chr8:4644739-4644789	Caco-2	colon:	n/a
45	chr8:4573688-4573738	AG04449	skin:	fetal
46	chr8:4573688-4573738	A549	lung:	n/a
47	chr8:4583355-4583405	Hepatocyte	liver:	n/a
48	chr8:4583355-4583405	HCPEpiC	choroid plexus:	n/a
49	chr8:4601508-4601558	A549	lung:	n/a
50	chr8:4629524-4629574	HMEC	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:30519178..30519958-chr8:4582339..4582839,2	MCF-7	breast:
2	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:
3	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-7	chr8:4644854-4646106	NONHSAT124751

No data

Variant related genes	Relation type
PAICSP4	TF binding region
PAICSP4	CpG island

Extended variants
information (count: 6237 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:6237 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78394611	chr8:4570602-4570603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531689993	chr8:4570649-4570650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1564181	chr8:4570655-4570656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs77936490	chr8:4570661-4570662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548016188	chr8:4570670-4570671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150454681	chr8:4570671-4570672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145293463	chr8:4570677-4570678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551065231	chr8:4570685-4570686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569665721	chr8:4570705-4570706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149193411	chr8:4570709-4570710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369592932	chr8:4570727-4570728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567024222	chr8:4570737-4570738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534468764	chr8:4570748-4570749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552763139	chr8:4570755-4570756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373519847	chr8:4570759-4570760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577487965	chr8:4570772-4570773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183462606	chr8:4570781-4570782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190417832	chr8:4570783-4570784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143374827	chr8:4570790-4570791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375072837	chr8:4570792-4570793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182348730	chr8:4570795-4570796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376478671	chr8:4570797-4570798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562119792	chr8:4570799-4570800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529418286	chr8:4570802-4570803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567550805	chr8:4570814-4570815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541606465	chr8:4570817-4570818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560012180	chr8:4570822-4570823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533440449	chr8:4570826-4570827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186955352	chr8:4570827-4570828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569546034	chr8:4570848-4570849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191736210	chr8:4570849-4570850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538599501	chr8:4570851-4570852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558674891	chr8:4570858-4570859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56219712	chr8:4570867-4570868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs534433038	chr8:4570877-4570878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138286438	chr8:4570896-4570897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200854200	chr8:4570897-4570898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528671074	chr8:4570919-4570920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552726883	chr8:4570931-4570932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs3031272	chr8:4570932-4570933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200198313	chr8:4570936-4570937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201209747	chr8:4570937-4570938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56295432	chr8:4570940-4570941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571143244	chr8:4570944-4570945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538548308	chr8:4570980-4570981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139374930	chr8:4570994-4570995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575454236	chr8:4570999-4571000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181502650	chr8:4571009-4571010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111783788	chr8:4571016-4571017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574156601	chr8:4571020-4571021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4570600-4586800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:4573000-4573200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr8:4573000-4573600	Enhancers	Fetal Heart	heart
4	chr8:4573200-4573600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:4573200-4573600	Enhancers	H9 Cell Line	embryonic stem cell
6	chr8:4573200-4573600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr8:4573200-4574000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:4573200-4574000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr8:4573200-4574000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:4573200-4574000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:4573200-4574200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr8:4573400-4573800	Enhancers	Brain Cingulate Gyrus	brain
13	chr8:4573400-4574000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr8:4573400-4574000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:4573400-4574000	Enhancers	Brain Substantia Nigra	brain
16	chr8:4573400-4574000	Enhancers	Fetal Lung	lung
17	chr8:4573400-4574200	Enhancers	Brain Hippocampus Middle	brain
18	chr8:4573600-4573800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:4573600-4574000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:4573600-4574200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:4573600-4574200	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr8:4586800-4587800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr8:4587800-4592600	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr8:4592400-4592800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr8:4592400-4593200	Enhancers	Colon Smooth Muscle	Colon
26	chr8:4592600-4593200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr8:4593200-4593600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr8:4593600-4593800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:4593800-4616600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr8:4597200-4597600	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr8:4597200-4598000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr8:4610600-4612600	Enhancers	Fetal Brain Male	brain
33	chr8:4611000-4611400	Enhancers	Stomach Smooth Muscle	stomach
34	chr8:4615000-4616800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr8:4616600-4617400	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:4616800-4617000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:4617000-4617200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:4617200-4617800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:4617400-4619600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr8:4617800-4619600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr8:4619600-4620200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr8:4619600-4620600	Enhancers	Brain Angular Gyrus	brain
43	chr8:4619600-4621000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:4619600-4623200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr8:4619800-4620400	Enhancers	Brain Hippocampus Middle	brain
46	chr8:4619800-4621000	Enhancers	Brain Substantia Nigra	brain
47	chr8:4620000-4620400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr8:4620000-4620400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr8:4620000-4620400	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr8:4620000-4621000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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